rs3091338
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3091338(C;C) |
| Make rs3091338(C;T) |
| Make rs3091338(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 132067045 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3091338 |
| dbSNP (classic) | rs3091338 |
| ClinGen | rs3091338 |
| ebi | rs3091338 |
| HLI | rs3091338 |
| Exac | rs3091338 |
| Gnomad | rs3091338 |
| Varsome | rs3091338 |
| LitVar | rs3091338 |
| Map | rs3091338 |
| PheGenI | rs3091338 |
| Biobank | rs3091338 |
| 1000 genomes | rs3091338 |
| hgdp | rs3091338 |
| ensembl | rs3091338 |
| geneview | rs3091338 |
| scholar | rs3091338 |
| rs3091338 | |
| pharmgkb | rs3091338 |
| gwascentral | rs3091338 |
| openSNP | rs3091338 |
| 23andMe | rs3091338 |
| SNPshot | rs3091338 |
| SNPdbe | rs3091338 |
| MSV3d | rs3091338 |
| GWAS Ctlg | rs3091338 |
| GMAF | 0.2094 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22412388 ]
|
| Trait | |
| Title | A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. |
| Risk Allele | T |
| P-val | 4E-8 |
| Odds Ratio | 1.2300 None |
